LP56779-9
Cystic fibrosis
Active
Description
An autosomal recessive genetic disease of the exocrine glands. It is caused by mutations in the gene encoding the cystic fibrosis transmembrane conductance regulator expressed in several organs including the lung, the pancreas, the biliary system, and the sweat glands. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in airway obstruction, chronic respiratory infections, pancreatic insufficiency, maldigestion, salt depletion, and heat prostration. Source: National Library of Medicine, MeSH 2006
Basic Part Properties
- Part Display Name
- Cystic fibrosis
- Part Type
- Component (Describes the core component or analyte measured)
- Created On
- 2006-09-01
- Construct for LOINC Short Name
- CF
LOINC Terminology Service (API) using HL7® FHIR® Get Info
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- CodeSystem lookup
- https:
//fhir.loinc.org/CodeSystem/$lookup?system=http: //loinc.org&code=LP56779-9
Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| zh-CN | Chinese (China) | 囊性纤维化 Synonyms: CF; |
| fr-CA | French (Canada) | Mucovscidose |
| et-EE | Estonian (Estonia) | Tsüstiline fibroos |
| es-ES | Spanish (Spain) | Fibrosis quística |
| it-IT | Italian (Italy) | Fibrosi cistica |
| tr-TR | Turkish (Turkey) | Kistik fibrozis |
| ru-RU | Russian (Russian Federation) | Кистозный фиброз Synonyms: Муковисцидоз |
| nl-NL | Dutch (Netherlands) | cystische fibrose Synonyms: cystic fibrosis; |
| fr-BE | French (Belgium) | Mucovscidose |
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